Works matching Fetal growth disorders


Results: 999
    1
    2
    3
    4

    Neurodevelopment at 2 years and umbilical artery Doppler in cases of very preterm birth after prenatal hypertensive disorder or suspected fetal growth restriction: EPIPAGE-2 prospective population-based cohort study.

    Published in:
    2020
    By:
    • Delorme, P.;
    • Kayem, G.;
    • Lorthe, E.;
    • Sentilhes, L.;
    • Zeitlin, J.;
    • Subtil, D.;
    • Rozé, J. C.;
    • Vayssière, C.;
    • Durox, M.;
    • Ancel, P. Y.;
    • Pierrat, V.;
    • Goffinet, F.;
    • Arnaud, Catherine;
    • Blanc, Julie;
    • Boileau, Pascal;
    • Debillon, Thierry;
    • D'Ercole, Claude;
    • Desplanches, Thomas;
    • Diguisto, Caroline;
    • Foix‐L'Hélias, Laurence
    Publication type:
    journal article
    5
    6
    7
    8
    9
    10
    11
    12
    13
    14
    15
    16
    17
    18
    19
    20
    21
    22
    23
    24
    25
    26
    27
    28
    29
    30
    31

    Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population.

    Published in:
    NPJ Genomic Medicine, 2023, v. 8, n. 1, p. 1, doi. 10.1038/s41525-023-00353-0
    By:
    • Slavotinek, Anne;
    • Rego, Shannon;
    • Sahin-Hodoglugil, Nuriye;
    • Kvale, Mark;
    • Lianoglou, Billie;
    • Yip, Tiffany;
    • Hoban, Hannah;
    • Outram, Simon;
    • Anguiano, Beatrice;
    • Chen, Flavia;
    • Michelson, Jeremy;
    • Cilio, Roberta M.;
    • Curry, Cynthia;
    • Gallagher, Renata C.;
    • Gardner, Marisa;
    • Kuperman, Rachel;
    • Mendelsohn, Bryce;
    • Sherr, Elliott;
    • Shieh, Joseph;
    • Strober, Jonathan
    Publication type:
    Article
    32
    33
    34
    35
    36
    37
    38
    39
    40
    41
    42
    43
    44
    45
    46
    47
    48
    49

    Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci.

    Published in:
    Human Molecular Genetics, 2009, v. 18, n. 24, p. 4724, doi. 10.1093/hmg/ddp435
    By:
    • Azzi, Salah;
    • Rossignol, Sylvie;
    • Steunou, Virginie;
    • Sas, Theo;
    • Thibaud, Nathalie;
    • Danton, Fabienne;
    • Le Jule, Maryline;
    • Heinrichs, Claudine;
    • Cabrol, Sylvie;
    • Gicquel, Christine;
    • Le Bouc, Yves;
    • Netchine, Irene
    Publication type:
    Article
    50